Rouleau GA - Search Results

1

Recent advances in the genetics of distal hereditary motor neuropathy give insight to a disease mechanism involving copper homeostasis that may extend to other motor neuron disorders.

Merner ND, Dion PA, Rouleau GA. Merner ND, et al. Among authors: rouleau ga. Clin Genet. 2011 Jan;79(1):23-34. doi: 10.1111/j.1399-0004.2010.01591.x. Clin Genet. 2011. PMID: 21143467

2

CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation.

Gaspar C, Jannatipour M, Dion P, Laganière J, Sequeiros J, Brais B, Rouleau GA. Gaspar C, et al. Among authors: rouleau ga. Hum Mol Genet. 2000 Aug 12;9(13):1957-66. doi: 10.1093/hmg/9.13.1957. Hum Mol Genet. 2000. PMID: 10942424

3

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.

Daoud H, Valdmanis PN, Kabashi E, Dion P, Dupré N, Camu W, Meininger V, Rouleau GA. Daoud H, et al. Among authors: rouleau ga. J Med Genet. 2009 Feb;46(2):112-4. doi: 10.1136/jmg.2008.062463. Epub 2008 Oct 17. J Med Genet. 2009. PMID: 18931000

4

Mutations in FUS cause FALS and SALS in French and French Canadian populations.

Belzil VV, Valdmanis PN, Dion PA, Daoud H, Kabashi E, Noreau A, Gauthier J; S2D team; Hince P, Desjarlais A, Bouchard JP, Lacomblez L, Salachas F, Pradat PF, Camu W, Meininger V, Dupré N, Rouleau GA. Belzil VV, et al. Among authors: rouleau ga. Neurology. 2009 Oct 13;73(15):1176-9. doi: 10.1212/WNL.0b013e3181bbfeef. Epub 2009 Sep 9. Neurology. 2009. PMID: 19741216 Free PMC article.

5

Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death.

Fan X, Dion P, Laganiere J, Brais B, Rouleau GA. Fan X, et al. Among authors: rouleau ga. Hum Mol Genet. 2001 Oct 1;10(21):2341-51. doi: 10.1093/hmg/10.21.2341. Hum Mol Genet. 2001. PMID: 11689481

6

Lithium chloride attenuates cell death in oculopharyngeal muscular dystrophy by perturbing Wnt/β-catenin pathway.

Abu-Baker A, Laganiere J, Gaudet R, Rochefort D, Brais B, Neri C, Dion PA, Rouleau GA. Abu-Baker A, et al. Among authors: rouleau ga. Cell Death Dis. 2013 Oct 3;4(10):e821. doi: 10.1038/cddis.2013.342. Cell Death Dis. 2013. PMID: 24091664 Free PMC article.

7

Parkinson's Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder.

Gan-Or Z, Girard SL, Noreau A, Leblond CS, Gagnon JF, Arnulf I, Mirarchi C, Dauvilliers Y, Desautels A, Mitterling T, Cochen De Cock V, Frauscher B, Monaca C, Hogl B, Dion PA, Postuma RB, Montplaisir JY, Rouleau GA. Gan-Or Z, et al. Among authors: rouleau ga. J Mol Neurosci. 2015 Jul;56(3):617-22. doi: 10.1007/s12031-015-0569-7. Epub 2015 May 1. J Mol Neurosci. 2015. PMID: 25929833

8

PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophy.

Shanmugam V, Dion P, Rochefort D, Laganière J, Brais B, Rouleau GA. Shanmugam V, et al. Among authors: rouleau ga. Ann Neurol. 2000 Nov;48(5):798-802. Ann Neurol. 2000. PMID: 11079546

9

Schwannomin isoform-1 interacts with syntenin via PDZ domains.

Jannatipour M, Dion P, Khan S, Jindal H, Fan X, Laganière J, Chishti AH, Rouleau GA. Jannatipour M, et al. Among authors: rouleau ga. J Biol Chem. 2001 Aug 31;276(35):33093-100. doi: 10.1074/jbc.M105792200. Epub 2001 Jun 29. J Biol Chem. 2001. PMID: 11432873 Free article.

10

Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and Sweden.

Valdmanis PN, Kabashi E, Dyck A, Hince P, Lee J, Dion P, D'Amour M, Souchon F, Bouchard JP, Salachas F, Meininger V, Andersen PM, Camu W, Dupré N, Rouleau GA. Valdmanis PN, et al. Among authors: rouleau ga. Neurology. 2008 Aug 12;71(7):514-20. doi: 10.1212/01.wnl.0000324997.21272.0c. Neurology. 2008. PMID: 18695162

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